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Postganglionic Sudomotor Dysfunction and Brain Glucose Hypometabolism in Patients with Multiple System Atrophy
Seung Woo Kim1, Seok Jong Chung1,2, Sangwon Lee3
1Department of Neurology, Yonsei University College of Medicine, Seoul, South Korea.
Sudomotor dysfunction, assessed by quantitative sudomotor axon reflex testing (QSART), is linked to increased disease severity in multiple system atrophy (MSA) patients. Abnormal QSART results correlate with higher Unified Multiple System Atrophy Rating Scale scores and greater neuropathological burden.
Area of Science:
- Neurology
- Autonomic Neuroscience
Background:
- Sudomotor dysfunction is a frequent complication in multiple system atrophy (MSA).
- This dysfunction stems from the degeneration of sympathetic neurons and postganglionic fibers, measurable via quantitative sudomotor axon reflex testing (QSART).
Purpose of the Study:
- To investigate the association between abnormal QSART responses and disease severity in patients with MSA.
- To explore the relationship between sudomotor function, overall disease burden, and neuroimaging findings.
Main Methods:
- A retrospective study included probable MSA patients who underwent 18F-FDG-PET/CT and autonomic function tests.
- Autonomic function tests were scored for sudomotor, cardiovagal, and adrenergic functions, with sudomotor function assessed by QSART.
- Disease severity was evaluated using the Unified Multiple System Atrophy Rating Scale (UMSARS) Parts I, II, and I+II.
Main Results:
- Abnormal QSART results were observed in 62.2% of 74 MSA patients.
- Patients with abnormal QSART exhibited significantly higher UMSARS Part I+II scores.
- Regression analysis revealed significant associations between UMSARS Part I and II scores and the sudomotor sub-score, indicating a link between sudomotor function and disease severity.
- Abnormal QSART correlated with reduced metabolic activity in the cerebellum (MSA-P) and basal ganglia (MSA-C) on 18F-FDG-PET/CT.
Conclusions:
- Postganglionic sudomotor dysfunction in MSA patients is associated with greater disease severity.
- These patients may also exhibit a more significant neuropathological burden compared to those without sudomotor dysfunction.
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